510(k) K051773 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
MODEL 3873 1* 8 AND MODEL 3874 1* 8 COMPACT TEST STIMULATION LEADS
| Applicant | Medtronic Inc.,Neurological Division., Miinneapolis MN, US |
| Decision | Substantially Equivalent, Jul 28, 2005 |
| Received | Jul 1, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K051773
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.